SLAIN2

mutation — cross-omics
Cross-omicsMUTATION → RNAPatientPairwise association · TCGA cohorts

Across TCGA patient cohorts, SLAIN2 mutation is significantly associated with the RNA expression of many other genes, with 941 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLAIN2-associated genes across cancer lineages are MIR520C, RNU6-1318P, and RNA5SP164. Each is linked with SLAIN2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLAIN2-to-partner and partner-to-SLAIN2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR520C grouped by SLAIN2-low versus SLAIN2-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLAIN2→partner) and Y-score (partner→SLAIN2) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
BLCAMIR520C →+0.564+4.704<.001.00532
UCECRNU6-1318P →+0.284+2.658<.001.00532
UCECRNA5SP164 →+0.107+4.153<.001.00532
UCECRNU6-965P →+0.233+4.153<.001.00532
COADRNU6-7 →+0.382+4.173.005.00332
SKCMTEX36-AS1 →+0.041+4.624<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 941 associations by consensus.

MIR520C by SLAIN2 expression — BLCA

Box plot of MIR520C in SLAIN2-low vs SLAIN2-high samples in BLCA.

Explore this box plot interactively →

Exploration